Canonical Allele Identifier: CA1785189032

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54628096A= , CM000670.2:g.54628096A=	GRCh38
NC_000008.10:g.55540656A= , CM000670.1:g.55540656A=	GRCh37
NC_000008.9:g.55703209A=	NCBI36
NG_009840.1:g.17030A=
NG_009840.2:g.17030A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.4214A= MANE Select	ENSP00000220676.1:p.Glu1405=
ENST00000636932.1:c.787+5808A=	ENSP00000489857.1:n.787+5808A=
ENST00000637698.1:c.787+5808A=	ENSP00000490104.1:n.787+5808A=
ENST00000220676.1:c.4214A=	ENSP00000220676.1:p.Glu1405=
NM_006269.1:c.4214A=	NP_006260.1:p.Glu1405=
XM_017013721.1:c.4235A=	XP_016869210.1:p.Glu1412=
XM_017013722.1:c.4214A=	XP_016869211.1:p.Glu1405=
NM_001375654.1:c.787+5808A=	NP_001362583.1:n.787+5808A=
NM_006269.2:c.4214A= MANE Select	NP_006260.1:p.Glu1405=